Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Vandana Lal"'
Autor:
Deepak Panwar, Kumar Gautam Singh, Shruti Mathur, Bhagwati Prasad, Anita Joshi, Vandana Lal, Atul Thatai
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-6 (2022)
Abstract Background Tibial muscular dystrophy (TMD), tardive, is a dominantly inherited mild degenerative disorder of anterior tibial muscles. Mutations of Titin (TTN) have been reported in patients with different phenotypes such as skeletal muscular
Externí odkaz:
https://doaj.org/article/02d25d080fd5460bbb1835cf0bbb4c76
Autor:
Shiba Ranjan Mishra, Leena Rawal, Moneeb A. K. Othman, Atul Thatai, Aditi Sarkar, Vandana Lal, Saurabh Kumar Bhattacharya
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Background The translocation t(8;21)(q22;q22) is one of the most frequent chromosomal abnormalities associated with acute myeloid leukemia (AML) sub type M2. About 3–5 % of cases with additional chromosomal abnormalities, including structu
Externí odkaz:
https://doaj.org/article/568317231d6c4e6e9a135e040aac856e
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Background: Human reproduction is the most intricate event as ~ 20% of human pregnancies end in miscarriages for which chromosomal anomalies are a common factor. The chromosomal variations associated with reproductive failures include translocations,
Externí odkaz:
https://doaj.org/article/0fdbd24b1c23423c9e9aaf2f1546b3b2
Publikováno v:
American Journal of Microbiological Research. 10:50-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14e318087515aafd2a2e7cdb53c5071a
https://doi.org/10.12691/ajmr-10-2-1
https://doi.org/10.12691/ajmr-10-2-1
Publikováno v:
American Journal of Infectious Diseases and Microbiology. 8:132-138
Aims and objectives: The purpose of this study is to observe the recent prevalence to assess drug resistance pattern of Extremely-drug resistant (XDR) and Pan drug resistant (PDR) isolates of Acinetobacter baumanii and Pseudomonas aeruginosa among cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c33de1ed54e75b9189cdb9b209c16966
https://doi.org/10.12691/ajidm-8-4-3
https://doi.org/10.12691/ajidm-8-4-3
Publikováno v:
Journal of Human Reproductive Sciences
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Background: Human reproduction is the most intricate event as ~ 20% of human pregnancies end in miscarriages for which chromosomal anomalies are a common factor. The chromosomal variations associated with reproductive failures include translocations,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87e4c3880b9e572f6c0f69650da6868
http://europepmc.org/articles/PMC7727889
http://europepmc.org/articles/PMC7727889
Publikováno v:
Microbiology Research Journal International. :1-10
Background: Atypical bacterial and viral pathogens play an important role in atypical pneumonia are responsible for one of the leading causes of morbidity and mortality, particularly in developing countries. Objective: The purpose of this study to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3f7d3f1bde2c0c12c58f8fecea4daa2
https://doi.org/10.9734/mrji/2020/v30i630223
https://doi.org/10.9734/mrji/2020/v30i630223
BACKGROUND Alagille syndrome is an autosomal dominant disorder associated with variable clinical phenotypic features including cholestasis, congenital heart defects, vertebral defects, and dysmorphic facies. OBJECTIVE Whole exome sequencing (WES) has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de13d67ba08ef29815ea371fecc699c0
https://doi.org/10.2196/preprints.33946
https://doi.org/10.2196/preprints.33946
Publikováno v:
Asian Journal of Medicine and Health. :1-8
Aims and Objectives: This study was undertaken to highlight the resistance pattern of Nitrofurantoin among 5162 UTIs causing isolates at Microbiology Department of Dr. Lal Path Labs between April to June 2019. Materials and Methods: This retrospectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643e6e3bce03c9ea7efc48ed8eed43fc
https://doi.org/10.9734/ajmah/2019/v16i130134
https://doi.org/10.9734/ajmah/2019/v16i130134
Publikováno v:
JMIR Bioinformatics and Biotechnology. 3:e33946
Background Alagille syndrome is an autosomal dominant disorder associated with variable clinical phenotypic features including cholestasis, congenital heart defects, vertebral defects, and dysmorphic facies. Objective Whole exome sequencing (WES) has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb9af1cf51811b41d464b0603a0fb1c5
https://doi.org/10.2196/33946
https://doi.org/10.2196/33946